Furosemide - 55154-2391-8 - (Furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 55154-2391
Proprietary Name: Furosemide
Non Proprietary Name: Furosemide
Active Ingredient(s): 10    mg/mL & nbsp;   Furosemide
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Furosemide

Product NDC: 55154-2391
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018667
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20100713

Package Information of Furosemide

Package NDC: 55154-2391-8
Package Description: 1 VIAL in 1 BAG (55154-2391-8) > 10 mL in 1 VIAL

NDC Information of Furosemide

NDC Code 55154-2391-8
Proprietary Name Furosemide
Package Description 1 VIAL in 1 BAG (55154-2391-8) > 10 mL in 1 VIAL
Product NDC 55154-2391
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20100713
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Cardinal Health
Substance Name FUROSEMIDE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of Furosemide


General Information